US3968187A - Flame retardant haloalkyl esters of glycols - Google Patents

Flame retardant haloalkyl esters of glycols Download PDF

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US3968187A
US3968187A US05/318,448 US31844872A US3968187A US 3968187 A US3968187 A US 3968187A US 31844872 A US31844872 A US 31844872A US 3968187 A US3968187 A US 3968187A
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compounds
vinyl
glycol
bis
compound
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US05/318,448
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Albert W. Morgan
William Vanderlinde
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Monsanto Co
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Monsanto Co
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Priority to US05/318,448 priority Critical patent/US3968187A/en
Priority to CA187,139A priority patent/CA1009662A/en
Priority to BE138494A priority patent/BE808197A/en
Priority to FR7343773A priority patent/FR2211466B1/fr
Priority to AU63482/73A priority patent/AU6348273A/en
Priority to DE2362078A priority patent/DE2362078A1/en
Priority to GB5805173A priority patent/GB1452111A/en
Priority to JP49004731A priority patent/JPS4998092A/ja
Priority to US05/529,680 priority patent/US3976619A/en
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/51—Phosphorus bound to oxygen
    • C08K5/52—Phosphorus bound to oxygen only
    • C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/093—Polyol derivatives esterified at least twice by phosphoric acid groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
    • C07F9/165—Esters of thiophosphoric acids
    • C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl

Definitions

  • This invention relates to novel flame retardant compounds, flame retardant resin compositions containing same and to a method for imparting flame resistance to natural and synthetic resins.
  • this invention is directed to novel haloalkyl esters of glycols which have been found to impart flame resistance to a variety of polymeric materials.
  • U.S. Pat. No. 2,978,478 discloses that alkylene glycols may be reacted with phosphorus compounds, such as phosphorusoxychloride, to prepare phosphate esters.
  • phosphorus compounds such as phosphorusoxychloride
  • the reaction described in the patent is disclosed in the present invention as a method for preparing intermediate compounds which are subsequently converted to the novel flame retardant compounds of the present invention.
  • the patent advises against preparing phosphate esters by the glycol/phosphorus oxychloride reaction since it is stated that heterocyclic esters will result therefrom, as well as the formation of diphosphate and polyphosphate esters.
  • the patent does not disclose the compounds of the present invention.
  • U.S. Pat. No. 3,192,242 discloses certain bis (halo-methyl)- 1,3- propylenebis (phosphoroidihalidates) and reaction thereof with oxirane compounds to prepare flame retardant halogenated diphosphates.
  • the haloalkyl glycol esters of the present invention are not shown.
  • U.S. Pat. No. 3,360,591 discloses chlorine-substituted aromatic esters of aromatic glycols which are used to reduce preignition of fuels. The compounds of the present invention are not disclosed.
  • This invention relates to compounds of the formula ##EQU2## ,wherein R represents alkylene, cycloalkylene or bis (alkylene) cycloalkylene; R' represents an alkylene group of 1 to 10 carbon atoms; X represents oxygen or sulfur; hal represents chlorine or bromine and n represents an integer of from 0 to 5.
  • the compounds of the invention have utility as flame retardant materials for resins.
  • the objective of this invention is to provide novel flame retardant materials to provide resin compositions containing same and to also provide a method for imparting flame retardance to resin systems.
  • novel compounds of the invention are prepared by reacting phosphoroldihalidates of glycols or glycol ethers having the formula
  • Illustrative glycols which are utilized in the preparation of the compounds of the invention include alkylene glycols, cycloalalkylene glycols, bis (alkylene) cycloalkylene glycols and alkylene glycol ethers.
  • Illustrative alkylene glycols include alkylene glycols having from 1 to 10 carbon atoms, such as ethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, and decamethylene glycol.
  • Illustrative cycloalkylene glycols include cyclohexylene glycol (e.g. 1.4-cyclohexanediol) and cyclopentylene glycol and smilar compounds.
  • Illustrative glycol ethers include diethylene glycol, dipropylene glycol and the like.
  • the oxirane reactant which is utilized in the preparation of the compounds of the present invention includes ethylene oxide, 1,2-propylene oxide, mixtures of ethylene oxide and propylene oxide, styrene oxide, epoxyalkanes such as 1,2-epoxybutane and the like.
  • the phosphorus oxyhalide or thiohalide reactant which is utilized in the preparation of the compounds of the present invention includes phosphorus oxytrichloride, phosphorus oxytribromide, phosphorus oxydibromidechloride and the corresponding thiophosphorus analogs.
  • the compounds of the invention are prepared by initially reacting the desired glycol with a phosphorus oxyhalide or phosphorus thiohalide to afford the intermediate glycol phosphorodihalidate or thiophosphorodihalidate, which is subsequently reacted with an oxirane compound to obtain the compounds of the invention.
  • the reaction conditions under which the compounds of the present invention are prepared are applicable to either batch or continuous operation.
  • the temperature may be in the range of 0° to 100°C., with 40° to 60°C. preferable.
  • the reaction may be run under a vacuum, a slight pressure (i.e. 2-20 psi) is preferable. Standard purification work-up procedures are used.
  • Example 2 To the product of Example 1 there is added 2.5 gms. tetrabutyl titanate. Ethylene oxide is added subsurface at such a rate that the temperature is maintained at 65°-70°C. Completion of the reaction is indicated by an abrupt drop in temperature. The product is washed with sodium bicarbonate/water, dehydrated and filtered. The product is diethylene glycol bis-di-2-chloroethylphosphate. There is obtained 507 gms. (98 percent) of product.
  • Example 2 tetrabutyl titanate is added to the product of Example 3 and ethylene oxide is introduced.
  • the product is cyclohexane dimethylol-bis-di-2-chloroethylphosphate.
  • Example 2 In accordance with the procedure of Example 1, there are reacted one mole of 1,4-cyclohexanediol and two moles of phosphorus oxychloride to afford cyclohexanediol bis-phosphorodichloridate.
  • Example 2 tetrabutyl titanate is added to the product of Example 5 and ethylene oxide is introduced.
  • the product is cyclohexanediol-1,4-bis-di-2-chloroethylphosphate.
  • This example illustrates the flame retardant utility of the compounds of the present invention when incorporated in various resin composition.
  • a polymer composition is prepared having the following formulation:Substituent Parts by Weight________________________________”EPI-REZ” 1 70.0"VERSAMID” 2 30.0"MODAFLOW” 3 0.3Flame Retardant 5, 10 or 20______________________________________ 1 "EPI-REZ” 510 - epoxy resin presently available from Celanese Chemical Co. 2 "VERSAMID” - polyamide stabilizer presently available from General Mills. 3 "MODAFLOW” - processing aid presently available from Monsanto Company.
  • the comparative properties of the resins are shown in Table I, below.
  • the "oxygen index" reflects data obtained in accordance with ASTM D2863-70 and is defined as the minimum concentration of oxygen, expressed as volume percent, in a mixture of oxygen and nitrogen that will just support combustion under the conditions of the test procedure. The greater the oxygen index, the better the flame retardancy.
  • Example 2 The compound of Example 2 demonstrates improved flame retardance.
  • the column marked "ASTM-D-1962" in Table II refers to a horizontal burning test for cellular plastics.
  • a specimen (6 inches ⁇ 2 inches ⁇ 1/2 inch) is supported on a horizontal, hard-cloth support with the 1/2 inch dimension vertical.
  • One end of the specimen is contacted for 60 seconds with a 11/21/2 inch high blue flame from a 3/8 inch diameter barrel Bunsen burner fitted with a 17/8 inch wide wingtop.
  • the specimen instantly goes out, it is self-extinguishing. If the specimen burns and subsequently goes out, it is characterized as self-extinguishing/burn rate given as inches and seconds burned. If the specimen completely burns, its burn rate in inches/minute is given.
  • Fire retardants incorporated in flexible urethane foam are often so volatile as to be unusable in practical applications.
  • Table II the compound of Example 2 renders the foam self-extinguishing with only a slight increase in volatility. It also processes with no internal discoloration or scorch. Ethylene glycol polyphosphate has been found to scorch in this formulation and, while rated self-extinguishing, is twice as volatile as the compound of Example 2.
  • the compounds of the present invention are useful as flame retardants for a wide variety of natural and synthetic polymer materials.
  • the compounds may be used in concentrations of from about 0.1 percent by weight of polymer up to about 50 weight percent or more depending on the particular use for which the polymer material is intended.
  • Synthetic polymer materials i.e., those high molecular weight organic materials which are not found in nature, with which the compounds of the invention are advantageously employed may be either linear or crosslinked polymers and may be in the form of sheets, coatings, foams and the like. They may be either those which are produced by addition or condensation polymerization.
  • An important class of polymers which are beneficially flame retarded with the compounds of the invention are those obtained from a polymerizable monomer compound having ethylenic unsaturation.
  • Compounds having such a radical are, for example, the solid polymeric alkenes, such as polyethylene, polypropylene, polyisobutylene or ethylene/propylene copolymers; polymerized acrylyl and alkacrylyl compounds such as acrylic, fluoroacrylic and methacrylic acids, anhydrides, esters.
  • nitriles and amides for example, acrylonitrile, ethyl or butyl acrylate, methyl or ethyl methacrylate, methoxymethyl or 2-(2-butoxyethoxyl)ethyl methacrylate, 2-cyanoethoxy)ethyl 3-(3-cyanopropoxy)propyl acrylate or methacrylate, 2(diethylamino)ethyl or 2-chloroethyl acrylate or methacrylate, acrylic anhydride or methacrylic anhydride; methacrylamide or chloroacrylamide; ethyl or butyl chloroacrylate; the olefinic aldehydes such as acrolein, methacrolein and their acetals; the vinyl and vinylidene halides such as vinyl chloride, vinyl fluoride, vinylidene fluoride and 1-chloro-1-fluoroethylene; polyvinyl alcohol; the vinyl carboxylates such as
  • Homopolymers of the above compounds or copolymers and terpolymers thereof are beneficially flame retarded by the compounds of the present invention.
  • Examples of such copolymers or terpolymers are those obtained by polymerization of the following monomer mixtures; vinyl chloride/vinyl acetate, ethylene/vinyl chloride/vinyl acetate, acrylonitrile/vinyl pyridine, styrene/methyl methacrylate, styrene/N-vinyl pyrrolidone, cyclohexyl methacrylate/vinyl chloroacetate, acrylonitrile/vinylidene cyanide, methyl methacrylate/vinyl acetate, ethyl acrylate/methacrylamide/ethyl chloroacrylate, vinyl chloride/vinylidene chloride/vinyl acetate.
  • Examples of particularly useful polymers and terpolymers prepared from the alpha-, betaolefinic dicarboxylic compounds are the copolymers of maleic anhydride and a vinyl compound such as ethylene, propylene, isobutylene, styrene, alpha methylstyrene, vinyl acetate, vinyl propionate, methyl isopropenyl ketone, isobutyl vinyl ether, the copolymers of dialkyl fumarate such as ethyl or butyl fumarate and vinyl compounds such as styrene, vinyl acetate, vinylidene chloride, ethyl methacrylate, acrylonitrile and the like.
  • a vinyl compound such as ethylene, propylene, isobutylene, styrene, alpha methylstyrene, vinyl acetate, vinyl propionate, methyl isopropenyl ketone, isobutyl vinyl ether
  • the compounds of the invention act as flame retardants for the polymers and copolymers of unsaturated, cyclic esters of carbonic acid, for example, homopolymeric vinylene carbonate or the copolymers of vinylene carbonate with ethylenic compounds such as ethylene, vinyl chloride, vinyl acetate, 1,3-butadiene, acrylonitrile, methacrylonitrile, or the esters of methacrylic or acrylic acid.
  • ethylenic compounds such as ethylene, vinyl chloride, vinyl acetate, 1,3-butadiene, acrylonitrile, methacrylonitrile, or the esters of methacrylic or acrylic acid.
  • Readily flame retarded by the compounds of the invention are also the polyarylcarbonate polymers such as the linear polyarylcarbonates formed from diphenols or dihydroxy aromatic compounds including single and fused-ring nucleii with two hydroxy groups as well as monohydroxy-substituted aromatic residues jointly in pairs by various connecting linkages.
  • polyarylcarbonate polymers such as the linear polyarylcarbonates formed from diphenols or dihydroxy aromatic compounds including single and fused-ring nucleii with two hydroxy groups as well as monohydroxy-substituted aromatic residues jointly in pairs by various connecting linkages.
  • Examples of the foregoing include dihydroxy benzenes, naphthalenes and the like, the dihydroxydiphenyl ethers, sulfones, alkanes, ketones and the like.
  • the compounds of the invention also act as flame retardants for polymers, copolymers or terpolymers of polymerizable compounds having a plurality of double bonds, for example, rubbery, conjugated diene polymerizates such as homopolymerized 3-butadiene, 2-chlorobutadiene or isoprene and linear copolymers or terpolymers such as butadiene/acrylonitrile, isobutylene/butadiene, butadiene/styrene; esters of saturated di- or poly-hydroxy compounds with olefinic carboxylic acids such as ethylene glycol dimethacrylate, triethylene glycol dicrotonate or glyceryl triacrylate; esters of olefinic alcohols with dicarboxylic acids or with olefinic monocarboxylic acids such as diallyl adipate, divinyl succinate, diallyl fumarate, allyl methacrylate or crotyl acrylate and other diethy
  • the compounds of the present invention are compatible flame retardants for epoxy resins.
  • resins are condensation products formed by the reaction of a polyhydroxy compound and epichlorohydrin, which condensation products are subsequently cured by the addition of crosslinking agents.
  • the hydroxy compounds may be, for example, ethylene glycol, 4,4'-isopropylidenediphenol and similar materials.
  • the crosslinking agent employed in the curing step may be a dicarboxylic compound such as phthalic anhydride or adipic acid, but is more generally a polyamine such as ethylene diamine, paraphenylamine diamine or diethylene triamine.
  • Polyurethanes are a class of polymer materials which are flame retarded by the compounds of the present invention.
  • the polyurethanes like the above-mentioned polyesters, are materials which are employed in structural applications, for example, as insulating foams, in the manufacture of textile fibers, as resin bases in the manufacture of curable coating compositions and as impregnating adhesives in the fabrication of laminates of wood and other fibrous materials.
  • the polyurethanes are condensation products of a diisocyanate and a compound having a molecular weight of at least 500 and preferably about 1,500-5,000 and at least two reactive hydrogen ions.
  • the useful active-hydrogen containing compounds may be polyesters prepared from polycarboxylic acids and polyhydric alcohols, polyhydric polyalkylene ethers having at least two hydroxy groups, polythioether glycols, polyesteramides and similar materials.
  • polyesters or polyester amides used for the production of the polyurethane may be branched and/or linear, for example, the esters of adipic, sebasic, 6-aminocaproic, phthalic, isophthalic, terephthalic, oxalic, malonic, succinic, maleic, cyclohexane-1,2-dicarboxylic, cyclohexane-1,4-dicarboxylic, polyacrylic, naphthalene1,2-dicarboxylic, fumaric or itaconic acids with polyalcohols such as ethylene glycol, diethylene glycol, pentaglycol, glycerol, sorbitol, triethanolamine and/or amino alcohols such as ethanolamine, 3-aminopropanol, and with mixtures of the above polyalcohols and amines.
  • polyalcohols such as ethylene glycol, diethylene glycol, pentaglycol, glycerol, sorbitol, tri
  • alkylene glycols and polyoxyalkylene or polythioalkylene glycols used in the production of polyurethanes may be ethylene glycol, propylene glycol, butylene glycol, diethylene glycol, triethylene glycol, polythioethylene glycol, dipropylene glycol and the like.
  • any of the polyesters, polyisocyanate-modified polyesters, polyester amides, polyisocyanate-modified polyester-amides, alkylene glycols, polyisocyanate-modified alkylene glycols, polyoxyalkylene glycols and polyisocyanate-modified polyoxyalkylene glycols having three reactive hydrogen atoms, three reactive carboxylic and/or especially hydroxyl groups may be employed in the production of polyurethanes.
  • any organic compound containing at least two radicals selected from the group consisting of hydroxy and carboxy groups may be employed.
  • Phenolic resins are flame retarded by the compounds of the present invention, which compounds may be incorporated into the phenolic resin either by milling and molding applications or by addition to film-forming or impregnating and bonding solutions prior to casting.
  • Phenolic resins with which the present compounds are employed are, for example, the phenol-aldehyde resins prepared from phenols such as phenol, cresol, xylenol, resorcinol, 4-butylphenyl, cumylphenol, 4-phenylphenol, nonylphenol, and aldehydes such as formaldehyde, acetaldehyde or butyraldehyde in the presence of either acetic or basic catalysts, depending upon whether the resin is intended for use as a molding or extruding resin or as the resin base in coating and impregnating compositions.
  • Aminoplasts are another group of aldehyde resins which are flame retarded by the compounds of the invention.
  • Examples of aminoplasts are the heat-convertible condensation products of an aldehyde with urea, thiourea, guanidine, cyanamide, dicyandiamide, alkyl or aryl guanamines and the triazines such as melamine, 2-fluoro-4,6-diamino-1,3,5-triazine and the like.
  • the aminoplasts are to be used as impregnating agents, bonding adhesives, coatings and in casting of films, the compounds of the present invention are incorporated into solutions or suspensions in which the aminoplast is carried. The resulting mixtures give strong, fire-retardant laminates when sheets of paper, glass, cloth or fabric are impregnated therewith and cured.
  • nylons for example, the superpolyamides which are generally obtained by the condensation of a diamine, for example, hexamethylene diamine with a dicarboxylic acid, for example, adipic acid.
  • polyamides which are flame retarded in accordance with the present invention are the polypeptides which may be prepared, for example, by reaction of N-carbobenzyl oxyglycine with glycine or mixture of glycine and lysine or an N-carboxy amino acid anhydride such as N-carboxy-DL-phenylalanine anhydride, piperidone, 2-oxohexamethyleneimine and other cyclic amides.
  • the compounds of the present invention can be incorporated into molding or extruding compositions for a flame retardant effect.
  • the preferred synthetic polymer materials which are flame retarded by the compounds of the present invention are the vinyl halide polymers in the form of milled products, plastisols and foams, rigid and flexible polyurethane coatings and foams, epoxy resins, ABS and GRS rubbers, aminoplasts and phenolics.
  • the vinyl halide polymers can be simple, mixed homopolymers of vinyl chloride or polyvinylidene chloride, or copolymers or terpolymers in which the essential polymeric structure of polyvinyl chloride is interspersed at intervals with residues of other ethylenically unsaturated compounds copolymerizable therewith.
  • the essential properties of the polymeric structure of polyvinyl chloride is retained if not more than about 40 percent of a comonomer is copolymerized therewith.
  • Especially preferred copolymers include ethylene/vinyl chloride and vinyl chloride/acrylonitrile copolymers.
  • Especially preferred terpolymers include ethylene/vinyl chloride/acrylonitrile, ethylene/vinyl chloride/acrylic acid and ethylene/vinyl chloride/acrylamide terpolymers.
  • Natural polymeric materials which may be flame retarded by the compounds of the present invention include natural rubber, cellulose esters, for example, cellulose acetate and cellulose nitrate, ethyl cellulose, cork and wood flour products and similar cellulosic materials.
  • polymer formulations which are flame retarded in accordance with the present invention may contain various conventional additives such as fillers, extenders, crosslinking agents and colorants. Minor amounts of stabilizers, for example, are usually incorporated to reduce the effects of heat and light.
  • the composition When foamable compositions are used, the composition may be a self-blowing polymer or the polymer may be blown by chemical or mechanical means or by the use of compressed gas.
  • Fillers which are frequently employed to lower the cost of the finished material and to modify its properties include calcium carbonate and magnesium silicate. When fillers are employed, they are generally present in an amount of up to about 150 parts by weight of filler per 100 parts by weight of polymer formulation.
  • colorants or color-pigments are incorporated in amounts of from about one to about five parts by weight to 100 parts by weight of polymer.
  • glass-forming inorganic materials such as zinc borate, zinc oxide, lead oxide, lead silicate and silicon dioxide may be added to decrease the flame and smoke generating characteristics of the polymer.

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Abstract

Compound of the formula ##EQU1## WHEREIN R represents alkylene, cycloalkylene or alkylenecycloalkylene, R' represents an alkylene group of 1 to 10 carbons, X represents oxygen or sulfur, hal represents chlorine or bromine and n represents an integer from zero to 5, are useful as flame retardants for material and synthetic material.

Description

BACKGROUND OF THE INVENTION
This invention relates to novel flame retardant compounds, flame retardant resin compositions containing same and to a method for imparting flame resistance to natural and synthetic resins.
More particularly, this invention is directed to novel haloalkyl esters of glycols which have been found to impart flame resistance to a variety of polymeric materials.
PRIOR ART
Prior art which appears relevant to the present invention is as follows:
U.S. Pat. No. 2,978,478 discloses that alkylene glycols may be reacted with phosphorus compounds, such as phosphorusoxychloride, to prepare phosphate esters. The reaction described in the patent is disclosed in the present invention as a method for preparing intermediate compounds which are subsequently converted to the novel flame retardant compounds of the present invention. The patent advises against preparing phosphate esters by the glycol/phosphorus oxychloride reaction since it is stated that heterocyclic esters will result therefrom, as well as the formation of diphosphate and polyphosphate esters. The patent does not disclose the compounds of the present invention.
U.S. Pat. No. 3,192,242 discloses certain bis (halo-methyl)- 1,3- propylenebis (phosphoroidihalidates) and reaction thereof with oxirane compounds to prepare flame retardant halogenated diphosphates. The haloalkyl glycol esters of the present invention are not shown.
U.S. Pat. No. 3,360,591 discloses chlorine-substituted aromatic esters of aromatic glycols which are used to reduce preignition of fuels. The compounds of the present invention are not disclosed.
SUMMARY OF THE INVENTION
This invention relates to compounds of the formula ##EQU2## ,wherein R represents alkylene, cycloalkylene or bis (alkylene) cycloalkylene; R' represents an alkylene group of 1 to 10 carbon atoms; X represents oxygen or sulfur; hal represents chlorine or bromine and n represents an integer of from 0 to 5. The compounds of the invention have utility as flame retardant materials for resins.
The objective of this invention is to provide novel flame retardant materials to provide resin compositions containing same and to also provide a method for imparting flame retardance to resin systems.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The objective of this invention is accomplished by providing compounds of formula (I) above.
The novel compounds of the invention are prepared by reacting phosphoroldihalidates of glycols or glycol ethers having the formula
HO-R --OR).sub.n OH                                        II
,wherein R and n are defined above with respect to Formula (I), with an oxirane compound.
Illustrative glycols which are utilized in the preparation of the compounds of the invention include alkylene glycols, cycloalalkylene glycols, bis (alkylene) cycloalkylene glycols and alkylene glycol ethers.
Illustrative alkylene glycols include alkylene glycols having from 1 to 10 carbon atoms, such as ethylene glycol, tetramethylene glycol, pentamethylene glycol, hexamethylene glycol, and decamethylene glycol.
Illustrative cycloalkylene glycols include cyclohexylene glycol (e.g. 1.4-cyclohexanediol) and cyclopentylene glycol and smilar compounds.
Illustrative bis (alkylene) cycloalkylene glycols include bis (methylene) cyclohexylene glycol (e.g. 1.4-cyclohexane dimethylol), bis (ethylene) cyclohexylene glycol, bis (propylene) cyclohexylene glycol and like compounds.
Illustrative glycol ethers include diethylene glycol, dipropylene glycol and the like.
The preferred glycols and glycol ethers which are utilized to prepare the flame retardant materials of the present invention include diethylene glycol, ethylene glycol, cyclohexane dimethylol and cyclohexanediol.
The oxirane reactant which is utilized in the preparation of the compounds of the present invention include diethylene glycol, ethylene glycol, cyclohexane dimethylol and cyclohexane diol.
The oxirane reactant which is utilized in the preparation of the compounds of the present invention includes ethylene oxide, 1,2-propylene oxide, mixtures of ethylene oxide and propylene oxide, styrene oxide, epoxyalkanes such as 1,2-epoxybutane and the like.
The phosphorus oxyhalide or thiohalide reactant which is utilized in the preparation of the compounds of the present invention includes phosphorus oxytrichloride, phosphorus oxytribromide, phosphorus oxydibromidechloride and the corresponding thiophosphorus analogs.
Generally, the compounds of the invention are prepared by initially reacting the desired glycol with a phosphorus oxyhalide or phosphorus thiohalide to afford the intermediate glycol phosphorodihalidate or thiophosphorodihalidate, which is subsequently reacted with an oxirane compound to obtain the compounds of the invention.
The reaction conditions under which the compounds of the present invention are prepared are applicable to either batch or continuous operation. The temperature may be in the range of 0° to 100°C., with 40° to 60°C. preferable. Although the reaction may be run under a vacuum, a slight pressure (i.e. 2-20 psi) is preferable. Standard purification work-up procedures are used.
Fire retardant properties are afforded in natural and synthetic polymer materials by incorporating the compounds of the invention into such materials in an amount of from 1 to 100 phr (parts per hundred resin), preferably in an amount of from about 3 to about 20 phr.
The following examples illustrate specific embodiments of the preparation and utility of certain of the compounds of the present invention.
EXAMPLE 1 Preparation of Diethylene Glycol Bis-phosphorodichloridate
In a one liter flask, fitted with a mechanical stirrer, thermometer and reflux condenser are placed 307 gms. (2.0 moles) phosphorus oxychloride. The phosphorus oxychloride is cooled to 14° to 15°C. and 106 gms. (1.0 moles) of diethylene glycol is added over a period of 2 to 3 hours. Residual phosphorus oxychloride is removed. The product recovered is diethylene glycol bis-phosphorodichloridate. The temperature of the reaction mixture is then raised to 30°C. for about one hour.
EXAMPLE 2 Preparation of Diethylene Glycol Bis-di-2-chloroethylphosphate
To the product of Example 1 there is added 2.5 gms. tetrabutyl titanate. Ethylene oxide is added subsurface at such a rate that the temperature is maintained at 65°-70°C. Completion of the reaction is indicated by an abrupt drop in temperature. The product is washed with sodium bicarbonate/water, dehydrated and filtered. The product is diethylene glycol bis-di-2-chloroethylphosphate. There is obtained 507 gms. (98 percent) of product.
EXAMPLE 3 Preparation of Cyclohexane Dimethylol-1,4-bis-phosphorodichloridate
In accordance with the procedure of Example 1, there are reacted one mole of cyclohexane dimethanol and two moles phosphorusoxychloride. The product is cyclohexane dimethylol-bis-phosphorodichloridate.
EXAMPLE 4 Preparation of Cyclohexane Dimethylol-bis-di-2-chloroethylphosphate
In accordance with the procedure of Example 2, tetrabutyl titanate is added to the product of Example 3 and ethylene oxide is introduced. The product is cyclohexane dimethylol-bis-di-2-chloroethylphosphate.
Following the procedure of Examples 1-4, but substituting phosphorus thiochloride for phosphorus oxychloride there is obtained diethylene glycol bis-thiophosphorodichloridate, diethylene glycol bis-di-2-chloroethylthiophosphate, cyclohexane dimethylol bis-thiophosphorodichloridate and cyclohexane dimethylol bis-di-2-chloroethylthiophosphate.
Substitution of propylene oxide for ethylene oxide in Examples 2 and 4 affords diethylene glycol bis-di-2-chloropropylphosphate and cyclohexanedimethylol bis-di-2-chloropropylphosphate.
EXAMPLE 5 Preparation of Cyclohexanediol Bis-phosphorodichloridate
In accordance with the procedure of Example 1, there are reacted one mole of 1,4-cyclohexanediol and two moles of phosphorus oxychloride to afford cyclohexanediol bis-phosphorodichloridate.
EXAMPLE 6 Preparation of Cyclohexanediol--1,4-bis-di-2-chloroethylphosphate
In accordance with the procedure of Example 2, tetrabutyl titanate is added to the product of Example 5 and ethylene oxide is introduced. The product is cyclohexanediol-1,4-bis-di-2-chloroethylphosphate.
EXAMPLE 7
This example illustrates the flame retardant utility of the compounds of the present invention when incorporated in various resin composition.
A polymer composition is prepared having the following formulation:Substituent Parts by Weight______________________________________"EPI-REZ"1 70.0"VERSAMID"2 30.0"MODAFLOW"3 0.3Flame Retardant 5, 10 or 20______________________________________ 1 "EPI-REZ" 510 - epoxy resin presently available from Celanese Chemical Co. 2 "VERSAMID" - polyamide stabilizer presently available from General Mills. 3 "MODAFLOW" - processing aid presently available from Monsanto Company.
Three formulations are prepared, one being a control, the second containing a commerical flame retardant ("FYROL" 99, a trademark of Stauffer Chemical Co. for their brand of ethylene glycol polyphosphate flame retardant) and the third containing the compound of Example 2 of the invention. The comparative properties of the resins are shown in Table I, below. The "oxygen index " reflects data obtained in accordance with ASTM D2863-70 and is defined as the minimum concentration of oxygen, expressed as volume percent, in a mixture of oxygen and nitrogen that will just support combustion under the conditions of the test procedure. The greater the oxygen index, the better the flame retardancy.
                                  Table I                                 
__________________________________________________________________________
                                      Water Extraction                    
                           Oxygen     48 Hrs. Drying                      
                    Volatility,                                           
                           Index,                                         
                               % Soluble                                  
                                      &                                   
Flame Retardant PHR*                                                      
                    % Loss % O.sub.2                                      
                               Mat. Loss                                  
                                      Absorption                          
__________________________________________________________________________
Control         0   0.11   17.9                                           
                               0      1.89                                
Ethylene glycol polyphosphate                                             
                5   0.59   21.2                                           
                               0      3.22                                
                10  0.03   21.2                                           
                               0.05   3.96                                
Example 2       5   0.46   21.6                                           
                               0      3.04                                
Compound**      10  0.03   21.3                                           
                               0.56   4.12                                
__________________________________________________________________________
 *PHR - parts per hundred resin                                           
 **Diethylene glycol bis-di-2-chloroethyl phosphate
The compound of Example 2 demonstrates improved flame retardance.
EXAMPLE 8
The compound of Example 2 is formulated, at 15 phr, into a flexible urethane foam having the following formulation:
Substituent            Parts by Weight                                    
______________________________________                                    
Polyoxypropylene glycol                                                   
                       100.00                                             
Triethylenediamine     0.65                                               
Silicon surfactant     1.00                                               
Water                  4.00                                               
Stannous octoate stabilizer                                               
                       0.16                                               
Tolylene diisocyanate  54.00                                              
______________________________________
The properties of the formulation are tested in comparison to a control containing no flame retardant and in comparison to the formulation containing 15 phr of a commercial flame retardant. The data are shown in Table II, below.
The column marked "ASTM-D-1962" in Table II refers to a horizontal burning test for cellular plastics. In such test, a specimen (6 inches × 2 inches × 1/2 inch) is supported on a horizontal, hard-cloth support with the 1/2 inch dimension vertical. One end of the specimen is contacted for 60 seconds with a 11/21/2 inch high blue flame from a 3/8 inch diameter barrel Bunsen burner fitted with a 17/8 inch wide wingtop.
If the specimen instantly goes out, it is self-extinguishing. If the specimen burns and subsequently goes out, it is characterized as self-extinguishing/burn rate given as inches and seconds burned. If the specimen completely burns, its burn rate in inches/minute is given.
              Table II                                                    
______________________________________                                    
Flame     Rate     Self-Exting.      Volatility                           
Retardant In./Min. In.     Sec. Fogging                                   
                                       % Loss                             
______________________________________                                    
Control   6.8      --      --   99     0.20                               
Example 2                                                                 
Compound  --       0.5     10   89     0.77                               
Ethylene                                                                  
glycol                                                                    
polyphosphate                                                             
          --       0.5     11   44     1.43                               
______________________________________
Fire retardants incorporated in flexible urethane foam are often so volatile as to be unusable in practical applications. In Table II the compound of Example 2 renders the foam self-extinguishing with only a slight increase in volatility. It also processes with no internal discoloration or scorch. Ethylene glycol polyphosphate has been found to scorch in this formulation and, while rated self-extinguishing, is twice as volatile as the compound of Example 2.
Results comparable to Examples 7 and 8 are obtained when the compounds of the present invention are incorporated in other resin systems, e.g. methacrylates, melamine/formaldehyde, vinyl halides and the like as described hereinafter.
As illustrated in Examples 7 and 8, the compounds of the present invention are useful as flame retardants for a wide variety of natural and synthetic polymer materials. The compounds may be used in concentrations of from about 0.1 percent by weight of polymer up to about 50 weight percent or more depending on the particular use for which the polymer material is intended.
Synthetic polymer materials, i.e., those high molecular weight organic materials which are not found in nature, with which the compounds of the invention are advantageously employed may be either linear or crosslinked polymers and may be in the form of sheets, coatings, foams and the like. They may be either those which are produced by addition or condensation polymerization.
An important class of polymers which are beneficially flame retarded with the compounds of the invention are those obtained from a polymerizable monomer compound having ethylenic unsaturation. A particularly preferred class of polymers which are flame retarded consist of the polymerized vinyl and vinylidene compounds, i.e., those having the CH2 = C< radical. Compounds having such a radical are, for example, the solid polymeric alkenes, such as polyethylene, polypropylene, polyisobutylene or ethylene/propylene copolymers; polymerized acrylyl and alkacrylyl compounds such as acrylic, fluoroacrylic and methacrylic acids, anhydrides, esters. nitriles and amides, for example, acrylonitrile, ethyl or butyl acrylate, methyl or ethyl methacrylate, methoxymethyl or 2-(2-butoxyethoxyl)ethyl methacrylate, 2-cyanoethoxy)ethyl 3-(3-cyanopropoxy)propyl acrylate or methacrylate, 2(diethylamino)ethyl or 2-chloroethyl acrylate or methacrylate, acrylic anhydride or methacrylic anhydride; methacrylamide or chloroacrylamide; ethyl or butyl chloroacrylate; the olefinic aldehydes such as acrolein, methacrolein and their acetals; the vinyl and vinylidene halides such as vinyl chloride, vinyl fluoride, vinylidene fluoride and 1-chloro-1-fluoroethylene; polyvinyl alcohol; the vinyl carboxylates such as vinyl acetate, vinyl chloroacetate, vinyl propionate, and vinyl 2-ethylhexanoate; the N-vinyl imides such as N-vinyl phthalimide and N-vinyl succinamide; the N-vinyl lactams such as N-vinyl caprolactam and N-vinyl butyrolactam; vinyl aromatic hydrocarbon compounds such as styrene, alpha-methylstyrene, 2,4dichlorostyrene, alpha- or beta-vinyl-naphthalene, divinyl benzene and vinyl fluorene; the vinyl ethers such as ethyl vinyl ether or isobutyl vinyl ether; vinyl-substituted heterocyclic compounds such as vinyl pyridine, vinyl pyrrolidone, vinylfuran or vinylthiophene; the vinyl or vinylidene ketones such as methyl vinyl ketone or isopropenyl ethyl ketone; vinylidene cyanide. Homopolymers of the above compounds or copolymers and terpolymers thereof are beneficially flame retarded by the compounds of the present invention. Examples of such copolymers or terpolymers are those obtained by polymerization of the following monomer mixtures; vinyl chloride/vinyl acetate, ethylene/vinyl chloride/vinyl acetate, acrylonitrile/vinyl pyridine, styrene/methyl methacrylate, styrene/N-vinyl pyrrolidone, cyclohexyl methacrylate/vinyl chloroacetate, acrylonitrile/vinylidene cyanide, methyl methacrylate/vinyl acetate, ethyl acrylate/methacrylamide/ethyl chloroacrylate, vinyl chloride/vinylidene chloride/vinyl acetate.
Other polymers of compounds having the ethylenic group, >C = C<, are homopolymers, copolymers and terpolymers of the alpha-, beta-olefinic dicarboxylic acids and derivatives thereof such as the anhydrides, esters, amides, nitriles and imides, for example, methyl, butyl, 2-ethylhexyl or dodecyl fumarate or maleate; maleic chloromaleic, citraconic or itaconic anhydride; fumaronitrile, dichlorofumaronitrile or citracononitrile; fumaramide, maleamide or N-phenyl maleamide. Examples of particularly useful polymers and terpolymers prepared from the alpha-, betaolefinic dicarboxylic compounds are the copolymers of maleic anhydride and a vinyl compound such as ethylene, propylene, isobutylene, styrene, alpha methylstyrene, vinyl acetate, vinyl propionate, methyl isopropenyl ketone, isobutyl vinyl ether, the copolymers of dialkyl fumarate such as ethyl or butyl fumarate and vinyl compounds such as styrene, vinyl acetate, vinylidene chloride, ethyl methacrylate, acrylonitrile and the like.
The compounds of the invention act as flame retardants for the polymers and copolymers of unsaturated, cyclic esters of carbonic acid, for example, homopolymeric vinylene carbonate or the copolymers of vinylene carbonate with ethylenic compounds such as ethylene, vinyl chloride, vinyl acetate, 1,3-butadiene, acrylonitrile, methacrylonitrile, or the esters of methacrylic or acrylic acid.
Readily flame retarded by the compounds of the invention are also the polyarylcarbonate polymers such as the linear polyarylcarbonates formed from diphenols or dihydroxy aromatic compounds including single and fused-ring nucleii with two hydroxy groups as well as monohydroxy-substituted aromatic residues jointly in pairs by various connecting linkages. Examples of the foregoing include dihydroxy benzenes, naphthalenes and the like, the dihydroxydiphenyl ethers, sulfones, alkanes, ketones and the like.
The compounds of the invention also act as flame retardants for polymers, copolymers or terpolymers of polymerizable compounds having a plurality of double bonds, for example, rubbery, conjugated diene polymerizates such as homopolymerized 3-butadiene, 2-chlorobutadiene or isoprene and linear copolymers or terpolymers such as butadiene/acrylonitrile, isobutylene/butadiene, butadiene/styrene; esters of saturated di- or poly-hydroxy compounds with olefinic carboxylic acids such as ethylene glycol dimethacrylate, triethylene glycol dicrotonate or glyceryl triacrylate; esters of olefinic alcohols with dicarboxylic acids or with olefinic monocarboxylic acids such as diallyl adipate, divinyl succinate, diallyl fumarate, allyl methacrylate or crotyl acrylate and other diethylenically unsaturated compounds such as diallyl carbonate, divinyl ether or divinylbenzene, as well as the crosslinked polymeric materials such as methyl methacrylate/diallyl methacrylate copolymer or butadiene/styrene/divinyl benzene terpolymer.
The cellulose derivatives are flame retarded by the compounds of the present invention. For example, cellulose esters such as cellulose acetate, cellulose triacetate or cellulose butyrate, the cellulose ethers such as methyl or ethyl cellulose, cellulose nitrate, carboxymethyl cellulose, cellophane, rayon, regenerated rayon and the like may be flame retarded.
The compounds of the present invention are well suited for flame retarding liquid resin compositions of the polyester type, for example, the linear polyesters which are obtained by the reaction of one or more polyhydric alcohols with one or more alpha, beta-unsaturated polycarboxylic acids alone or in combination with one or more saturated polycarboxylic acid compounds, or the crosslinked polyester resins which are obtained by reacting a linear polyester with a compound containing a CH2 = C< group.
The compounds of the present invention are compatible flame retardants for epoxy resins. Such resins are condensation products formed by the reaction of a polyhydroxy compound and epichlorohydrin, which condensation products are subsequently cured by the addition of crosslinking agents. The hydroxy compounds may be, for example, ethylene glycol, 4,4'-isopropylidenediphenol and similar materials. The crosslinking agent employed in the curing step may be a dicarboxylic compound such as phthalic anhydride or adipic acid, but is more generally a polyamine such as ethylene diamine, paraphenylamine diamine or diethylene triamine.
Polyurethanes are a class of polymer materials which are flame retarded by the compounds of the present invention. The polyurethanes, like the above-mentioned polyesters, are materials which are employed in structural applications, for example, as insulating foams, in the manufacture of textile fibers, as resin bases in the manufacture of curable coating compositions and as impregnating adhesives in the fabrication of laminates of wood and other fibrous materials. Essentially, the polyurethanes are condensation products of a diisocyanate and a compound having a molecular weight of at least 500 and preferably about 1,500-5,000 and at least two reactive hydrogen ions. The useful active-hydrogen containing compounds may be polyesters prepared from polycarboxylic acids and polyhydric alcohols, polyhydric polyalkylene ethers having at least two hydroxy groups, polythioether glycols, polyesteramides and similar materials.
The polyesters or polyester amides used for the production of the polyurethane may be branched and/or linear, for example, the esters of adipic, sebasic, 6-aminocaproic, phthalic, isophthalic, terephthalic, oxalic, malonic, succinic, maleic, cyclohexane-1,2-dicarboxylic, cyclohexane-1,4-dicarboxylic, polyacrylic, naphthalene1,2-dicarboxylic, fumaric or itaconic acids with polyalcohols such as ethylene glycol, diethylene glycol, pentaglycol, glycerol, sorbitol, triethanolamine and/or amino alcohols such as ethanolamine, 3-aminopropanol, and with mixtures of the above polyalcohols and amines.
The alkylene glycols and polyoxyalkylene or polythioalkylene glycols used in the production of polyurethanes may be ethylene glycol, propylene glycol, butylene glycol, diethylene glycol, triethylene glycol, polythioethylene glycol, dipropylene glycol and the like.
Generally, any of the polyesters, polyisocyanate-modified polyesters, polyester amides, polyisocyanate-modified polyester-amides, alkylene glycols, polyisocyanate-modified alkylene glycols, polyoxyalkylene glycols and polyisocyanate-modified polyoxyalkylene glycols having three reactive hydrogen atoms, three reactive carboxylic and/or especially hydroxyl groups may be employed in the production of polyurethanes. Moreover, any organic compound containing at least two radicals selected from the group consisting of hydroxy and carboxy groups may be employed.
The organic polyisocyanates useful for the production of polyurethanes include ethylene diisocyanate, ethylidene diisocyanate, propylene-1,2-diisocyanate, m-phenylene diisocyanate, 2,4-tolylene diisocyanate, triphenylmethane triisocyanate, or polyisocyanates in blocked or inactive form such as the bis-phenyl carbamates of tolylene diisocyanate and the like.
Phenolic resins are flame retarded by the compounds of the present invention, which compounds may be incorporated into the phenolic resin either by milling and molding applications or by addition to film-forming or impregnating and bonding solutions prior to casting. Phenolic resins with which the present compounds are employed are, for example, the phenol-aldehyde resins prepared from phenols such as phenol, cresol, xylenol, resorcinol, 4-butylphenyl, cumylphenol, 4-phenylphenol, nonylphenol, and aldehydes such as formaldehyde, acetaldehyde or butyraldehyde in the presence of either acetic or basic catalysts, depending upon whether the resin is intended for use as a molding or extruding resin or as the resin base in coating and impregnating compositions.
Aminoplasts are another group of aldehyde resins which are flame retarded by the compounds of the invention. Examples of aminoplasts are the heat-convertible condensation products of an aldehyde with urea, thiourea, guanidine, cyanamide, dicyandiamide, alkyl or aryl guanamines and the triazines such as melamine, 2-fluoro-4,6-diamino-1,3,5-triazine and the like. When the aminoplasts are to be used as impregnating agents, bonding adhesives, coatings and in casting of films, the compounds of the present invention are incorporated into solutions or suspensions in which the aminoplast is carried. The resulting mixtures give strong, fire-retardant laminates when sheets of paper, glass, cloth or fabric are impregnated therewith and cured.
Another class of compounds which are flame retarded by the compounds of the present invention are the nylons, for example, the superpolyamides which are generally obtained by the condensation of a diamine, for example, hexamethylene diamine with a dicarboxylic acid, for example, adipic acid.
Other polyamides which are flame retarded in accordance with the present invention are the polypeptides which may be prepared, for example, by reaction of N-carbobenzyl oxyglycine with glycine or mixture of glycine and lysine or an N-carboxy amino acid anhydride such as N-carboxy-DL-phenylalanine anhydride, piperidone, 2-oxohexamethyleneimine and other cyclic amides. The compounds of the present invention can be incorporated into molding or extruding compositions for a flame retardant effect.
The compounds of the present invention are also useful as flame retardants for linear polymers obtained by the self-condensation of bifunctional compounds, for example, the polyethers which are derived by the self-condensation of dihydric alcohols such as ethylene glycol, propylene glycol or hexamethylene glycol; the polyesters which are obtained by the self-condensation of hydroxy acids such as lactic acid or 4-hydroxybutric acid; the polyamides which are prepared by the self-condensation of aminocarboxylic acids such as 4-aminobutyric acid; the polyanhydrides which are formed by the self-condensation of dicarboxylic acids such as sebasic or adipic acid.
The preferred synthetic polymer materials which are flame retarded by the compounds of the present invention are the vinyl halide polymers in the form of milled products, plastisols and foams, rigid and flexible polyurethane coatings and foams, epoxy resins, ABS and GRS rubbers, aminoplasts and phenolics. The vinyl halide polymers can be simple, mixed homopolymers of vinyl chloride or polyvinylidene chloride, or copolymers or terpolymers in which the essential polymeric structure of polyvinyl chloride is interspersed at intervals with residues of other ethylenically unsaturated compounds copolymerizable therewith. The essential properties of the polymeric structure of polyvinyl chloride is retained if not more than about 40 percent of a comonomer is copolymerized therewith. Especially preferred copolymers include ethylene/vinyl chloride and vinyl chloride/acrylonitrile copolymers. Especially preferred terpolymers include ethylene/vinyl chloride/acrylonitrile, ethylene/vinyl chloride/acrylic acid and ethylene/vinyl chloride/acrylamide terpolymers.
Natural polymeric materials which may be flame retarded by the compounds of the present invention include natural rubber, cellulose esters, for example, cellulose acetate and cellulose nitrate, ethyl cellulose, cork and wood flour products and similar cellulosic materials.
The polymer formulations which are flame retarded in accordance with the present invention, whether in sheet or film form or of foam or molded structure, may contain various conventional additives such as fillers, extenders, crosslinking agents and colorants. Minor amounts of stabilizers, for example, are usually incorporated to reduce the effects of heat and light.
When foamable compositions are used, the composition may be a self-blowing polymer or the polymer may be blown by chemical or mechanical means or by the use of compressed gas. Fillers which are frequently employed to lower the cost of the finished material and to modify its properties include calcium carbonate and magnesium silicate. When fillers are employed, they are generally present in an amount of up to about 150 parts by weight of filler per 100 parts by weight of polymer formulation.
Where a colored or tinted composition is desired, colorants or color-pigments are incorporated in amounts of from about one to about five parts by weight to 100 parts by weight of polymer.
Surfactants such as silicones are normally added to foam formulations which are mechanically frothed. The surfactants reduce the surface tension of the foam and thereby increase the air or gas entrapment characteristics of the foam.
Additionally, glass-forming inorganic materials such as zinc borate, zinc oxide, lead oxide, lead silicate and silicon dioxide may be added to decrease the flame and smoke generating characteristics of the polymer.
While the invention has been described by referring to certain specific embodiments, it is not so limited since many modifications and variations are possible in the light of the above teachings. The invention may therefore be practiced otherwise than as specifically described without departing from the spirit and scope of the invention.

Claims (5)

The embodiments in which an exclusive property or privilege is claimed are defined as follows:
1. A compound of the formula ##EQU3## wherein R represents cycloalkylene of 5 or 6 carbon atoms or alkylenecycloalkylene of 8, 10 or 12 carbon atoms, R' represents an alkylene group of 2 to 4 carbon atoms, X represents oxygen or sulfur, and hal represents chlorine or bromine.
2. Compound of claim 1 wherein R represents alkylenecycloalkylene.
3. Compound of claim 2 which is cyclohexane dimethylol bis-di-2-chloroethyl-phosphate.
4. Compound of claim 1 wherein R represents cycloalkylene.
5. Compound of claim 4 which is cyclohexanediol bis-di-2-chloroethyl phosphate.
US05/318,448 1972-12-26 1972-12-26 Flame retardant haloalkyl esters of glycols Expired - Lifetime US3968187A (en)

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US05/318,448 US3968187A (en) 1972-12-26 1972-12-26 Flame retardant haloalkyl esters of glycols
CA187,139A CA1009662A (en) 1972-12-26 1973-11-30 Flame retardant haloalkyl esters of glycols
BE138494A BE808197A (en) 1972-12-26 1973-12-04 HALOALKYL ESTERS OF FIRE-RESISTANT GLYCOLS
FR7343773A FR2211466B1 (en) 1972-12-26 1973-12-07
AU63482/73A AU6348273A (en) 1972-12-26 1973-12-11 Flame retardant haloalkyl esters of glycols
DE2362078A DE2362078A1 (en) 1972-12-26 1973-12-13 FIRE-RETARDANT HALOGENALKYLESTERS FROM GLYCOLS
GB5805173A GB1452111A (en) 1972-12-26 1973-12-14 Halogen-containing phosphate esters having flame retardant properties
JP49004731A JPS4998092A (en) 1972-12-26 1973-12-22
US05/529,680 US3976619A (en) 1972-12-26 1974-12-05 Flame retardant polymers containing phosphates

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4029721A (en) * 1974-10-26 1977-06-14 Hoechst Aktiengesellschaft Halogen-containing phosphoric acid polyesters
US4032498A (en) * 1974-10-24 1977-06-28 Hoechst Aktiengesellschaft Flame-retardant plasticizers for polyvinyl chloride
US4242138A (en) * 1975-07-31 1980-12-30 Sandoz Ltd. Flameproofed regenerated cellulose and method
US4246360A (en) * 1977-07-22 1981-01-20 Monsanto Company Fire retardant, non-dripping flexible polyurethane foam
US4278771A (en) * 1979-06-18 1981-07-14 Stauffer Chemical Company Flame retardant compositions
US4553713A (en) * 1983-06-21 1985-11-19 Gasway Corporation Coil winding control guide
US20030198823A1 (en) * 2001-12-05 2003-10-23 Isola Laminate Systems, Inc. Thermosetting resin composition for high performance laminates
US20100212540A1 (en) * 2007-10-02 2010-08-26 Solvay (Societe Anonyme) Use of compositions containing silicon for improving the corrosion resistance of vessels
CN107629085A (en) * 2017-09-19 2018-01-26 浙江万盛股份有限公司 A kind of post-processing approach of DECPP crude product

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5327643A (en) * 1976-08-27 1978-03-15 Asahi Glass Co Ltd Impartment of flame retardancy to phenolic resins
JP6635944B2 (en) * 2014-12-24 2020-01-29 大八化学工業株式会社 Flame retardant resin composition

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632767A (en) * 1948-12-29 1953-03-24 Standard Oil Dev Co Complex phosphate ester synthetic lubricant
US2782128A (en) * 1952-04-16 1957-02-19 Celanese Corp Plasticized cellulose acetate
US3707586A (en) * 1970-02-02 1972-12-26 Olin Corp Halogenated phosphate polyesters

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2036592C2 (en) * 1970-07-23 1984-05-10 Hoechst Ag, 6230 Frankfurt Means for reducing the flammability of polyurethane foams and processes for the production of flame-retardant polyurethane foams

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2632767A (en) * 1948-12-29 1953-03-24 Standard Oil Dev Co Complex phosphate ester synthetic lubricant
US2782128A (en) * 1952-04-16 1957-02-19 Celanese Corp Plasticized cellulose acetate
US3707586A (en) * 1970-02-02 1972-12-26 Olin Corp Halogenated phosphate polyesters

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Kosolapoff et al., Organic Phosphorus Compounds, vol. 6 (1973) p. 461. *
Piekos et al., Chemical Abstracts, vol. 58 (1963) 5496c. *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4032498A (en) * 1974-10-24 1977-06-28 Hoechst Aktiengesellschaft Flame-retardant plasticizers for polyvinyl chloride
US4029721A (en) * 1974-10-26 1977-06-14 Hoechst Aktiengesellschaft Halogen-containing phosphoric acid polyesters
US4242138A (en) * 1975-07-31 1980-12-30 Sandoz Ltd. Flameproofed regenerated cellulose and method
US4246360A (en) * 1977-07-22 1981-01-20 Monsanto Company Fire retardant, non-dripping flexible polyurethane foam
US4278771A (en) * 1979-06-18 1981-07-14 Stauffer Chemical Company Flame retardant compositions
US4553713A (en) * 1983-06-21 1985-11-19 Gasway Corporation Coil winding control guide
US20030198823A1 (en) * 2001-12-05 2003-10-23 Isola Laminate Systems, Inc. Thermosetting resin composition for high performance laminates
US7090924B2 (en) * 2001-12-05 2006-08-15 Isola Usa Corp. Thermosetting resin composition for high performance laminates
US20100212540A1 (en) * 2007-10-02 2010-08-26 Solvay (Societe Anonyme) Use of compositions containing silicon for improving the corrosion resistance of vessels
CN107629085A (en) * 2017-09-19 2018-01-26 浙江万盛股份有限公司 A kind of post-processing approach of DECPP crude product
CN107629085B (en) * 2017-09-19 2020-01-07 浙江万盛股份有限公司 Post-treatment method of diethylene glycol chloropropyl phosphate oligomer crude product

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JPS4998092A (en) 1974-09-17
BE808197A (en) 1974-06-04
DE2362078A1 (en) 1974-07-04

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